Posted , 13 users are following.
O my god that bloody. Needle nearly killed me !
I had a biopsy today , one in my LS area and one in an area that looked dodgy ..or whatever the Dr said
The DR practically confirmed I have LS just by looking and with the research I had done , I knew it was .
Although when researching the dreded 'C' word crops up a lot , so it has made me worry considerably ..
Anyway, when the DR said I need an additional biopsy , it has unsettled me a lot ..
Did this happen to many other people ?
And that flipping needle ..o my Lordy ..one in each side ..it was painful !
I'm really an others to hear others experiences ..
Sarah (42, warrington)
0 likes, 16 replies
If its any help, I know how you are feeling, lost, alone and terrified out of your wits.....XX
I hope you have had your mind put at rest somewhat since you last posted on here. I can only say to you that whilst there is a slightly increased risk of getting vulval cancer if you have LS, neverthless the chances are still very small. You just have to keep an eye on yourself for any changes without getting too worried about it. Of course it happens to some people so I really hope your second biopsy has shown nothing more than the LS by now. Not that 'just' the LS is a small thing but I hope you know what I mean. I'm tying myself in knots here. Along with lorna65 I know exactly how you are feeling. Do let us know how you are. I have to agree with you about how blooming painful the anasthetic needle for the LS biopsy in my inner labia was.
Good luck to you also lorna65
I have had LS for about 3-4 years, didn't feel I could talk to many people about this as I don't want to talk about my 'bits' with everyone! The biopsies were miserable. My husband doesn't fully understand but is very patient. It has changed our love life and my leisure.
I had just bought a horse ( just got to an age where we could afford it!) to share with my daughter and found it very painful to ride and have given up riding the last 2 years. But, having read the above feel a fraud and will stop moaning now.
But, if anyone has LS and still continues to ride a horse, please contact me, my daughter has just bought another horse and my old boy, now 22 (not my husband!) is available to ride again, she wants me to go on a 10 mile pleasure ride tomorrow! Will I be able to walk on Monday? Think not, just thinking of the pain lowering myself into the hot bath!
You are the first person that has the same problem as myself i.e. Raw burn type area, Private gynie said it was LS, then got an appointment at a Woman's clinic, consultant there said she didn't think it was LS, but wasn't sure what it was, so Biopsy on 10 th Oct .....Dermovate at night and in the morning it looks calm, but by night time, it is very red and raw looking again. This started with me 18 months ago and I am 65. Don't think I have shrinkage, but before this started I must admit I didn't look, however in the last 18 months, all has just stayed the same. Dermovate last thing at night certainly helps me, I have no problem sleeping, Every time I wee I make sure all residue is washed off. Hope this helps
I'm on Dermovate too so will see how it goes. I have another gynie appointment in six months but instructions on Dermovate say to use for eight weeks. Not sure how that will work out. The burn look isn't there all the time. Although I wake up at night with discomfort. Next appointment should be more helpful with information found on this site. Knowing what to ask sometimes is half the battle. Good luck with your biopsy in October at least you will know exactly what it is. Thanks for your help.
Cancer is rare and if you have the condition monitored regularly which is once or twice a year then it will be picked up and treated quickly.
Hang in there because with treatment your mind will be eased.
It is a horrible condition because it is something you don't want to talk about in mixed company or even amongst friends most of the time.
If it were on your hand you could show it and gain sympathy but this is such a hidden ailment it makes it much harder to vent about it.
All the best and keep your chin up!
Afterwards the hospital said that she couldn't leave the gel on long (for some reason) but she could have explained this to me at the time. Her bedside manner was awful. There HAS to be a better way of numbing this area and making the process more bearable. Admittedly once the anesthetic was in, I felt nothing.
My new consultant (a lovely lady) has been working with LS for years and hasn't yet seen a case of cancer; so I hope that is reassuring to others. Be aware too that post menopausal women can get atrophy. This has made my LS symptoms worse, or at least confused them. Be sure to get diagnosed properly. I was making an area just inside alot worse by continuing with steroid cream when it was probably caused by atrophy. When I started local hormone cream for the atrophy, the horrible soreness caused by over use of the steroid cream started to ease. Good luck everyone dealing with this. Sadly what with menopause, atrophy and LS, I've pretty much said goodbye to my sex-life!
Well , I had a labia removal , which was connected to poor stiches after childbirth 23 yrs ago, I'm 42.
The operation failed , all 40 stiches bust open and I had a major infection, 3 antibiotics later , reflux, constipation, ongoing LS, oral thrush , ulcers and general pain !
I have been to the hospital 10 times this month and my LS is bloody awful as I could not use my cream !
But.. Had sex twice ..was quite drunk though !
I'm doing back as a man !
Join this discussion or start a new one?New discussion Reply